Incidental Mutation 'IGL01795:4930451G09Rik'
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Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4930451G09Rik
Ensembl Gene ENSMUSG00000022543
Gene NameRIKEN cDNA 4930451G09 gene
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.080) question?
Stock #IGL01795
Quality Score
Chromosomal Location4968936-4978962 bp(+) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) T to G at 4974071 bp
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000090457]
Predicted Effect noncoding transcript
Transcript: ENSMUST00000090457
SMART Domains Protein: ENSMUSP00000087942
Gene: ENSMUSG00000022543

Pfam:DUF4701 1 195 7.5e-72 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000229669
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930572O03Rik C A 5: 15,656,886 probably benign Het
4930590J08Rik C T 6: 91,918,112 R263* probably null Het
Arfgef1 A T 1: 10,147,528 I1562K probably benign Het
B4galt1 T A 4: 40,807,760 D347V probably damaging Het
Ccdc178 T A 18: 22,019,118 R646S probably benign Het
Ccr1 A T 9: 123,964,112 L127* probably null Het
Cd109 A G 9: 78,661,765 probably benign Het
Chd6 A G 2: 160,961,374 V2128A probably benign Het
Chil6 T A 3: 106,388,792 I376F probably damaging Het
Chit1 T C 1: 134,148,429 S275P probably damaging Het
Erap1 T A 13: 74,666,090 probably null Het
F5 T C 1: 164,194,390 V1478A probably benign Het
Fras1 G T 5: 96,778,045 V3703F probably damaging Het
Hmmr C T 11: 40,721,734 M185I probably benign Het
Kcnu1 A G 8: 25,913,705 Y8C probably damaging Het
Krt16 A G 11: 100,247,724 probably benign Het
Mcf2l A G 8: 13,000,749 probably null Het
Mgat5 C T 1: 127,469,231 R572W probably damaging Het
Neil2 T C 14: 63,188,750 D57G probably benign Het
Nom1 A G 5: 29,446,871 T736A probably benign Het
Olfr1030 T A 2: 85,984,134 I98N probably damaging Het
Olfr1301 A T 2: 111,754,386 M46L probably benign Het
Olfr414 A T 1: 174,430,649 I74F possibly damaging Het
Prr14l A T 5: 32,831,845 probably benign Het
Sall1 A G 8: 89,028,680 S1224P probably benign Het
Slc44a2 A C 9: 21,345,349 K336Q probably damaging Het
Sptan1 C T 2: 30,018,489 T1754I probably benign Het
Zdhhc5 T C 2: 84,690,046 S596G probably benign Het
Other mutations in 4930451G09Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03052:4930451G09Rik APN 16 4977494 splice site noncoding transcript
R0392:4930451G09Rik UTSW 16 4977499 splice site noncoding transcript
R4851:4930451G09Rik UTSW 16 4976274 exon noncoding transcript
R5562:4930451G09Rik UTSW 16 4974076 exon noncoding transcript
R5868:4930451G09Rik UTSW 16 4974068 exon noncoding transcript
Posted On2014-02-04